ClinVar Miner

Submissions for variant NM_001166108.2(PALLD):c.1965-12569G>A

gnomAD frequency: 0.00007  dbSNP: rs568490721
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000527996 SCV000656945 likely benign Pancreatic adenocarcinoma 2024-01-06 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003952886 SCV004768807 likely benign PALLD-related disorder 2021-12-17 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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